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(1S,3AS,5R,6R,6AS)-1,6-DIALLYL-5-[(TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-HEXAHYDROPENTALEN-2(1H)-ONE

Compound with spectra: 1 NMR

(1S,3AS,5R,6R,6AS)-1,6-DIALLYL-5-[(TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-HEXAHYDROPENTALEN-2(1H)-ONE
SpectraBase Compound ID FsJ22JJ2GkR
InChI InChI=1S/C30H38O2Si/c1-6-14-25-27(31)20-22-21-28(26(15-7-2)29(22)25)32-33(30(3,4)5,23-16-10-8-11-17-23)24-18-12-9-13-19-24/h6-13,16-19,22,25-26,28-29H,1-2,14-15,20-21H2,3-5H3/t22-,25+,26-,28+,29+/m0/s1
InChIKey UKWUAKKQAYYMSX-CFVQQZOQSA-N
Mol Weight 458.7 g/mol
Molecular Formula C30H38O2Si
Exact Mass 458.264107 g/mol
Enantiomer InChIKey UKWUAKKQAYYMSX-JZFFRNTOSA-N

View Spectrum of (1S,3AS,5R,6R,6AS)-1,6-DIALLYL-5-[(TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-HEXAHYDROPENTALEN-2(1H)-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,3AS,4R,5R,6AS)-1,4-DIALLYL-5-[(TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-HEXAHYDROPENTALEN-2(1H)-ONE
[[(3AS,5R,6R,6AS)-6-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1,3A,4,5,6,6A-HEXAHYDROPENTALEN-2-YL]-OXY]-(TRIETHYL)-SILANE
5-[(1',1'-Dimethylethyl)diphenylsilyloxy]hexahydro-1-(1''-triethylsilyloxy-2"-octenyl)-2(1H)-pentalenone
(5E,1R*,2R*,4S*,8S*)-1-[(tert-Butyldimethylsilyl)oxy[-5-(cyclohexylmethylene)-2-[(phentlsilyl)methyl]bicyclo[4.3.0]nonane
(1R,3S,4S,5R)-3-[tert-butyl(diphenyl)silyl]oxy-4-methyl-5-(4-nitrophenyl)sulfonyloxy-1-cyclohexanecarboxylic acid methyl ester
(6R,8R)-8-((2R,4R,5R)-5-(2-(Benzyloxy)ethyl)-4-methyltetrahydrofuran-2-yl)-2,2,11,11-tetramethyl-3,3,10,10-tetraphenyl-4,9-dioxa-3,10-disiladodecan-6-yl isobutyrate
(1S)-1-(3"-Hydroxy-1"-octenyl)-5-[(1',1'-dimethylethyl)diphenylsilyloxy]octahydro-2-pentalenyl benzoate
(1R,2R,3aS,4aS)-2-t-Butyldiphenylsilyloxy-3a-carbomethoxy-1-ethylbicyclo[3.1.0]hexane
(1S,2R,3aS,4aS)-2-t-Butyldiphenylsilyloxy-1-ethyl-3a-carbomethoxybicyclo[3.1.0]hexane
Methyl (1R,3R)-2-[(t-butyldiphenylsilyl)oxy]-4-methylbicyclo[3.1.0]hexane-1-carboxylate
Title Journal or Book Year
Doing it Twice: Asymmetric Deprotonation/Alkylation of Weiss Diketone Derivatives as Key Steps in the Functionalization of Bicyclo[3.3.0]octanes European Journal of Organic Chemistry 2012
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